Canonical Allele Identifier: PA2826507510
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 139110
ClinVar RCV Id: RCV000128044 RCV000290434 RCV000476332 RCV001813391 RCV002399504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001255968.1:p.Ser486Gly
CA293486
NM_001269039.3:c.1456A>G